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Items: 1 to 20 of 232

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7046818inversion1nstd229human GRCh38 chr5: 79,066,734-79,366,047 , GRCh37.p13 chr5: 78,362,557-78,661,870 BHMT, DMGDH, 6 more genes
    nsv7045990inversion1nstd229human GRCh38 chr5: 78,952,825-79,153,510 , GRCh37.p13 chr5: 78,248,648-78,449,333 DMGDH, LOC100505796, 3 more genes
    nsv7045178inversion1nstd229human GRCh38 chr5: 79,128,001-79,128,088 , GRCh37.p13 chr5: 78,423,824-78,423,911 BHMT
    nsv7045119inversion1nstd229human GRCh38 chr5: 76,735,197-79,503,040 , GRCh37.p13 chr5: 76,031,022-78,798,863 RNU6ATAC36P, RPS3AP20, 39 more genes
    nsv7041510inversion1nstd229human GRCh38 chr5: 73,610,616-81,398,473 , GRCh37.p13 chr5: 72,906,441-80,694,292 LOC105379034, RBMX2P5, 134 more genes
    nsv7038776inversion1nstd229human GRCh38 chr5: 76,735,364-79,502,930 , GRCh37.p13 chr5: 76,031,189-78,798,753 HOMER1, LOC100505796, 39 more genes
    nsv6778008copy number variation1nstd229human GRCh38 chr5: 79,020,101-79,156,200 , GRCh37.p13 chr5: 78,315,924-78,452,023 BHMT2, BHMT, 1 more genes
    nsv6777538copy number variation1nstd229human GRCh38 chr5: 79,113,831-79,115,413 , GRCh37.p13 chr5: 78,409,654-78,411,236 BHMT
    nsv6777330copy number variation1nstd229human GRCh38 chr5: 79,123,740-79,129,032 , GRCh37.p13 chr5: 78,419,563-78,424,855 BHMT
    nsv6776694copy number variation1nstd229human GRCh38 chr5: 79,123,701-79,129,000 , GRCh37.p13 chr5: 78,419,524-78,424,823 BHMT
    nsv6775582copy number variation1nstd229human GRCh38 chr5: 79,081,601-79,283,300 , GRCh37.p13 chr5: 78,377,424-78,579,123 BHMT, RPS3AP20, 3 more genes
    nsv6775147copy number variation1nstd229human GRCh38 chr5: 79,120,982-79,479,817 , GRCh37.p13 chr5: 78,416,805-78,775,640 RNY3P1, LOC107986426, 6 more genes
    nsv6773744copy number variation1nstd229human GRCh38 chr5: 79,055,295-79,193,466 , GRCh37.p13 chr5: 78,351,118-78,489,289 BHMT2, DMGDH, 2 more genes
    nsv6772553copy number variation1nstd229human GRCh38 chr5: 79,122,259-79,122,352 , GRCh37.p13 chr5: 78,418,082-78,418,175 BHMT
    nsv6769059copy number variation1nstd229human GRCh38 chr5: 79,091,886-79,128,282 , GRCh37.p13 chr5: 78,387,709-78,424,105 BHMT
    nsv6763423copy number variation1nstd229human GRCh38 chr5: 77,899,127-80,222,849 , GRCh37.p13 chr5: 77,194,951-79,518,668 RNU6-183P, ARSB, 34 more genes
    nsv6762162copy number variation1nstd229human GRCh38 chr5: 78,796,013-79,169,970 , GRCh37.p13 chr5: 78,091,836-78,465,793 BHMT, DMGDH, 4 more genes
    nsv6636260copy number variation1nstd102humanUncertain significance GRCh37 chr5: 77,746,948-79,089,197 , GRCh38.p12 chr5: 78,451,125-79,793,374 RPL29P15, LOC102724530, 18 more genes
    nsv6630443copy number variation1nstd224human GRCh37 chr5: 78,375,222-78,417,087 , GRCh38.p12 chr5: 79,079,399-79,121,264 BHMT2, BHMT
    nsv6562879inversion1nstd223human GRCh38 chr5: 78,952,820-79,153,510 , GRCh37.p13 chr5: 78,248,643-78,449,333 ARSB, BHMT, 3 more genes
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